Personalized drug combinations to overcome trastuzumab resistance in HER2-positive breast cancer

被引:39
|
作者
Vu, Thuy [1 ,2 ]
Sliwkowski, Mark X. [3 ]
Claret, Francois X. [1 ,2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77030 USA
[2] Univ Texas Houston, Grad Sch Biomed Sci, Expt Therapeut Acad Program, Houston, TX 77030 USA
[3] Genentech Inc, Res Oncol, San Francisco, CA 94080 USA
来源
关键词
Targeted therapy; Combination approaches; HER2-positive breast cancer; Trastuzumab resistance; GROWTH-FACTOR RECEPTOR; TYROSINE KINASE INHIBITOR; PHASE-II TRIAL; PLUS TRASTUZUMAB; AKT INHIBITOR; ADJUVANT TRASTUZUMAB; MONOCLONAL-ANTIBODY; RAPAMYCIN INHIBITOR; TANESPIMYCIN; 17-AAG; ANTITUMOR EFFICACY;
D O I
10.1016/j.bbcan.2014.07.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
HER2-positive (HER2+) breast cancer accounts for 18%-20% of all breast cancer cases and has the second poorest prognosis among breast cancer subtypes. Trastuzumab, the first Food and Drug Administration-approved targeted therapy for breast cancer, established the era of personalized treatment for HER2+ metastatic disease. It is well tolerated and improves overall survival and time-to-disease progression: with chemotherapy, it is part of the standard of care for patients with HER2 + metastatic disease. However, many patients do not benefit from it because of resistance. Substantial research has been performed to understand the mechanism of trastuzumab resistance and develop combination strategies to overcome the resistance. In this review, we provide insight into the current pipeline of drugs used in combination with trastuzumab and the degree to which these combinations have been evaluated, especially in patients who have experienced disease progression on trastuzumab. We conclude with a discussion of the current challenges and future therapeutic approaches to trastuzumab-based combination therapy. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:353 / 365
页数:13
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